Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

Carbromal

From Wikipedia, the free encyclopedia

Carbromal
Skeletal formula of carbromal
Skeletal formula of carbromal
Names
IUPAC name
2-Bromo-N-carbamoyl-2-ethylbutanamide
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard100.000.952Edit this at Wikidata
EC Number
  • 201-046-6
KEGG
MeSHcarbromal
UNII
  • InChI=1S/C7H13BrN2O2/c1-3-7(8,4-2)5(11)10-6(9)12/h3-4H2,1-2H3,(H3,9,10,11,12) checkY
    Key: OPNPQXLQERQBBV-UHFFFAOYSA-N checkY
  • CCC(Br)(CC)C(=O)NC(N)=O
Properties
C7H13BrN2O2
Molar mass237.097 g·mol−1
AppearanceWhite crystals
OdorOdorless
Density1.544 g/cm3
Melting point119 °C (246 °F; 392 K)
Soluble
Solubilitysoluble inchloroform,ether,acetone,benzene
logP1.623
Acidity (pKa)10.69
Basicity (pKb)3.31
Structure
rhombic
Pharmacology
N05CM04 (WHO)
Related compounds
Related ureas
Bromisoval
Related compounds
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Carbromal is ahypnotic/sedative originally synthesized in 1909 by Bayer and subsequently marketed asAdalin.[1][2] The drug was later sold byParke-Davis in combination withpentobarbital, under the nameCarbrital.[3] As of 2015, it was still used in Hungary in combination withaminophenazone under the nameDemalgon.

Synthesis

[edit]
Carbromal synthesis:[2][4][5] Literature:[6][7]

Diethylmalonic acid [510-20-3] (1) is decarboxylated to 2-ethylvaleric acid [20225-24-5] (2). TheHell-Volhard-Zelinsky reaction converts this to 2-Bromo-2-Ethylbutyryl Bromide [26074-53-3] (3). Reaction withurea with affords carbromal (4).

See also

[edit]

References

[edit]
  1. ^Borrie P (March 1955)."A purpuric drug eruption caused by carbromal".British Medical Journal.1 (4914):645–6.doi:10.1136/bmj.1.4914.645.PMC 2061381.PMID 13230580.
  2. ^abDE 22571, "Verfahren dur Darstellung von Bromodiäthylacetylharnstoff [Method for the preparation of bromodiethylacetylurea]", published 1910-09-17, assigned toFriedrich Bayer & Co. 
  3. ^Physicians' Desk Reference (33 ed.). Oradell, N.J.: Medical Economics Co. 1979. p. 1266.ISBN 0-87489-999-0.OCLC 4636066.
  4. ^Frdl. 10, 1160
  5. ^Chem. Zentralbl. 1910, II, 1008.
  6. ^Slotta H (1931). Bauer KH (ed.).Grundriss der modernen Arzneistoff-Synthese. Stuttgart: Verlag Ferd. Enke.
  7. ^H. P. Kaufmann, Arzneimittel-Synthese (Berlin, 1953).
GABAA
Alcohols
Barbiturates
Benzodiazepines
Carbamates
Imidazoles
Monoureides
Neurosteroids
Nonbenzodiazepines
Phenols
Piperidinediones
Quinazolinones
Others
GABAB
H1
Antihistamines
Antidepressants
Antipsychotics
α2-Adrenergic
5-HT2A
Antidepressants
Antipsychotics
Others
Melatonin
Orexin
α2δVDCC
Others
Alcohols
Barbiturates
Benzodiazepines
Carbamates
Flavonoids
Imidazoles
Kava constituents
Monoureides
Neuroactive steroids
Nonbenzodiazepines
Phenols
Piperidinediones
Pyrazolopyridines
Quinazolinones
Volatiles/gases
Others/unsorted
Stub icon

Thissedative-related article is astub. You can help Wikipedia byexpanding it.

Retrieved from "https://en.wikipedia.org/w/index.php?title=Carbromal&oldid=1300897488"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp